Specific association of type I c-abl with ran GTPase in lipopolysaccharide-mediated differentiation

被引:6
作者
Daniel, R
Chung, SW
Eisenstein, TK
Sultzer, BM
Wong, PMC [1 ]
机构
[1] Temple Univ, Sch Med, Fels Inst Canc Res & Mol Biol, Dept Pathol & Lab Med, Philadelphia, PA 19140 USA
[2] Temple Univ, Sch Med, Fels Inst Canc Res & Mol Biol, Dept Microbiol & Immunol, Philadelphia, PA 19140 USA
[3] Stem Cell Therapeut, King Of Prussia, PA 19406 USA
关键词
Ran; LPS; endotoxin; sepsis; c-Abl isoform;
D O I
10.1038/sj.onc.1204361
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Each of several isoforms of c-Abl may be involved in different biological functions. Type I c-Abl has been shown to be involved in LPS-induced differentiation and Type IV c-Abl, apoptosis, Ran has recently been shown to be involved in LPS endotoxin signal transduction, Here we show that Type I c-Abl associates with Ran. Formation of this complex is specific, as Ran did not associate with the highly homologous Type IV c-Abl isoform, In non-stimulated lymphoid B cells, Type I c-Abl tyrosine kinase is inactive, whereas Type IV kinase is active. Formation of Type I c-Abl/Ran complex and activation of Type I c-Abl kinase activity are LPS dose-dependent. This complex is detectable in B cells of endotoxin-sensitive inbred mice but absent in B cells of endotoxin-resistant mice. These findings therefore suggest that Type I c-Abl and Ran are important targets in lipopolysaccharide-induced biological responses of hematopoietic cells.
引用
收藏
页码:2618 / 2625
页数:8
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